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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03355950
Other study ID # E-16-1019
Secondary ID
Status Recruiting
Phase N/A
First received January 30, 2017
Last updated November 22, 2017
Start date January 2017
Est. completion date August 2018

Study information

Verified date November 2017
Source Ankara Numune Training and Research Hospital
Contact Selami Ilgaz Kayilioglu, MD
Phone +90 533 203 6595
Email kayilioglu@yahoo.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine and compare the possible affects of two different inguinal hernia repair technique (TEP and Lichtenstein) on serum ASA levels.


Description:

Antisperm antibody levels are thought to be indirect indicators of spermatic duct injuries. The investigators' ultimate goal is to draw a conclusion about the effect of the type of surgery on spermatic duct integrity. The investigators are going to collect serum samples from inguinal hernia patients before and after surgery. The investigators aim to assess the effect of surgery on antisperm antibody levels of patients who undergo Licthenstein and TEP repair. Preoperative antisperm antibody levels will serve as control levels for each patient group.


Recruitment information / eligibility

Status Recruiting
Enrollment 160
Est. completion date August 2018
Est. primary completion date January 2018
Accepts healthy volunteers No
Gender Male
Age group 20 Years to 60 Years
Eligibility Inclusion Criteria:

- to accept the terms of the randomization and all study

- to have unilateral inguinal hernia and set for an inguinal hernia repair

- to be a father

Exclusion Criteria:

- to have any kind of autoimmune disorders

- any kind of infertility history

- to have a history of inguinal and/or genital surgery and/or trauma

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Lichtenstein Repair
Well defined Lichtenstein Repair for inguinal hernias
TEP Repair
Laparoscopic totally extraperitoneal repair for inguianal hernias

Locations

Country Name City State
Turkey Ankara Numune Training and Research Hospital Ankara

Sponsors (1)

Lead Sponsor Collaborator
Ankara Numune Training and Research Hospital

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change from baseline Anti-sperm antibody levels after inguinal hernia surgery Samples will be collected before hernia surgery and three months after surgery Three months for each patient
Secondary Comparison of Anti-sperm antibody levels between inguinal hernia patients who have undergone laparoscopic totally extraperitoneal repair and Lichtenstein repair techniques 2 years anticipated
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